rs878853376
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs878853376(A;T) |
Make rs878853376(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 11 |
Position | 77189468 |
Gene | MYO7A |
is a | snp |
is | mentioned by |
dbSNP | rs878853376 |
dbSNP (classic) | rs878853376 |
ClinGen | rs878853376 |
ebi | rs878853376 |
HLI | rs878853376 |
Exac | rs878853376 |
Gnomad | rs878853376 |
Varsome | rs878853376 |
LitVar | rs878853376 |
Map | rs878853376 |
PheGenI | rs878853376 |
Biobank | rs878853376 |
1000 genomes | rs878853376 |
hgdp | rs878853376 |
ensembl | rs878853376 |
geneview | rs878853376 |
scholar | rs878853376 |
rs878853376 | |
pharmgkb | rs878853376 |
gwascentral | rs878853376 |
openSNP | rs878853376 |
23andMe | rs878853376 |
SNPshot | rs878853376 |
SNPdbe | rs878853376 |
MSV3d | rs878853376 |
GWAS Ctlg | rs878853376 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs878853376(T;T) |
Alt | rs878853376(T;T) |
Reference | Rs878853376(A;A) |
Significance | Probable-Pathogenic |
Disease | Retinal dystrophy |
Variation | info |
Gene | MYO7A |
CLNDBN | Retinal dystrophy |
Reversed | 0 |
HGVS | NC_000011.9:g.76900513A>T |
CLNSRC | |
CLNACC | RCV000225423.1, |